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Journal of Lipid Research, Vol 35, 883-892, Copyright © 1994 by Lipid Research, Inc.
J Ko, JA Hamilton, HT Ton-Nu, CD Schteingart, AF Hofmann and DM Small
13C-NMR spectroscopy was used to examine the effect of side chain length on
the ionization properties and transmembrane transport rate of 3 alpha,7
alpha-dihydroxy bile acids. When solubilized in taurocholate micelles,
[23-13C]nor-chenodeoxycholic acid (nor-CDCA) had a pKa of 6.1, similar to
that of CDCA (pKa 6.2), its C24 homologue. In unilamellar
phosphatidylcholine vesicles, the pKa of nor-CDCA was 7.0, whereas that of
CDCA was 6.6. Lineshape analysis indicated that the rate of ionization of
nor-CDCA as a micellar solute or as a vesicle component was very slow (0.4
x 10(5) sec-1) compared to that of acetic acid in water (8.7 x 10(5)
sec-1). Lineshape analysis of spectra of the protonated form of nor-CDCA at
acidic bulk pH indicated that the transbilayer transport rate of nor-CDCA
(580 sec-1) was six times faster than that of CDCA (100 sec-1). It is
proposed that the shorter side chain of the nor-CDCA molecule causes it to
reside more deeply inside the vesicle bilayer than CDCA, explaining its
weaker ionization and more rapid flip-flop rate. These in vitro experiments
imply that, in vivo, a given C23 nor-dihydroxy bile acid will ionize less
readily when present in membranes, and it will also flip-flop faster than
its C24 homologue.
ARTICLES
Effects of side chain length on ionization behavior and transbilayer transport of unconjugated dihydroxy bile acids: a comparison of nor- chenodeoxycholic acid and chenodeoxycholic acid
Department of Biophysics, Housman Medical Research Center, Boston University School of Medicine, MA 02118.
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